COMPUTING RESOURCE ALLOCATION SCHEME OF IOV USING DEEP REINFORCEMENT LEARNING IN EDGE COMPUTING ENVIRONMENT



Morphofunctional rearrangement of the hepatic vasculature in the pathogenesis of portal hypertension in liver cirrhosis

The paper presents an update on the mechanisms for enhanced hepatic vascular resistance to the portal circulation underlying the pathogenesis of portal hypertension in liver General cirrhosis.In addition to gross hepatic structural disorders related to diffuse fibrosis and formation of regenerative nodules, the morphofunctional rearrangement of the

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(3R,4R,4aS,7aR,12bS)-3-Cyclopropylmethyl-4a,9-dihydroxy-3-methyl-7-oxo-2,3,4,4a,5,6,7,7a-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-3-ium bromide

The title compound, C21H26NO4+·Br−, also known as R-methylnaltrexone (MNTX) bromide, is a selective peripherally acting μ-opioid receptor antagonist with a oroxymorphone skeleton, General synthesized by hydroxyl protection, N-methylation, deprotection and anion exchange of naltrexone.It comprises a five-ring system A/B/C

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